CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 909 enrolled
Drug / intervention
Diclofenac Sodium 50Mg Suppository +1 moredrug
Likely dose
Diclofenac Sodium 50Mg Suppositoryfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03041779
NCT03041779Phase 2Completed
CompareCT.gov

A Single Blinded, Open-labelled, Randomized Control Trial Comparing Acetaminophen Rectal Suppository With Diclofenac Rectal Suppository as Analgesia for Perineal Injury Following Childbirth

Clinical Research Centre, Malaysia·interventional·Posted Feb 3, 2017·Updated Feb 3, 2017

In Brief

A Phase 2 clinical trial evaluating Diclofenac Sodium 50Mg Suppository and Paracetamol 500Mg Suppository for Perineal Tear and Perineal Laceration (Obstetric). Completed, enrolled 909 participants.

Detailed Summary

To assess the prevalence of pain score for perineum pain following childbirth followed by phase 2 study to assess the analgesic effectiveness of acetaminophen and diclofenac rectal suppository in postpartum perineum pain secondary to perineal trauma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPerineal Tear, Perineal Laceration (Obstetric)
Countries--
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 3, 2017
Enrollment StartOct 1, 2015
Primary CompletionJul 1, 2016
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 9.4 years ago

Interventions

Diclofenac Sodium 50Mg Suppositorydrug

Paracetamol 500Mg Suppositorydrug